A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557624



Internal ID330717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33911986..33981098hg38UCSC Ensembl
chr17:32239005..32308117hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3869113
hg1969113
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712729
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557624
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer